Diffusion of phenolic compounds through two high-density polyethylene geomembranes after 17 years under different exposure conditions

2016 ◽  
Vol 23 (5) ◽  
pp. 381-393 ◽  
Author(s):  
N. Touze-Foltz ◽  
M. Mendes ◽  
F. Farcas ◽  
L. Mazéas
2015 ◽  
Vol 52 (3) ◽  
pp. 326-343 ◽  
Author(s):  
R. Kerry Rowe ◽  
A.M.R. Ewais

The degradation of high-density polyethylene (HDPE) geomembranes exposed to the elements depends, inter alia, on the climatological conditions. This study investigates the degradation in the properties of HDPE geomembranes installed at two mine facilities after almost 16 years of exposure in a warm–hot climate and at a research site after 6 years of exposure in a mild–cold climate. Samples were exhumed at the field sites from different locations and the properties of the geomembrane were measured in the laboratory. The depletion of antioxidants detected by the standard oxidative induction time (Std-OIT) test for the geomembrane installed at the research site was faster on the slope than on the base; however, there was negligible difference in the depletion of antioxidants–stabilizers detected by the high-pressure oxidative induction time (HP-OIT) test between the slope and base. Under the field conditions described, the antioxidant depletion time for the exposed geomembrane installed at the research site (mild–cold climate) was inferred to be 20 to 54 years. The exposed HDPE geomembranes installed at the mine facilities (warm–hot climate) have reached the time of nominal failure based on their stress crack resistance. However, they have not ruptured under the exposure conditions even though the stress crack resistance has dropped to as low as 70 h at some locations.


2021 ◽  
Vol 121 ◽  
pp. 365-372
Author(s):  
Weishi Li ◽  
Ya Xu ◽  
Qifei Huang ◽  
Yuqiang Liu ◽  
Jingcai Liu

Antioxidants ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 14
Author(s):  
Sandra Rojas-Lema ◽  
Sergio Torres-Giner ◽  
Luis Quiles-Carrillo ◽  
Jaume Gomez-Caturla ◽  
Daniel Garcia-Garcia ◽  
...  

This study originally explores the use of naringin (NAR), gallic acid (GA), caffeic acid (CA), and quercetin (QUER) as natural antioxidants for bio-based high-density polyethylene (bio-HDPE). These phenolic compounds are present in various citrus fruits and grapes and can remain in their leaves, peels, pulp, and seeds as by-products or wastes after juice processing. Each natural additive was first melt-mixed at 0.8 parts per hundred resin (phr) of bio-HDPE by extrusion and the resultant pellets were shaped into films by thermo-compression. Although all the phenolic compounds colored the bio-HDPE films, their contact transparency was still preserved. The chemical analyses confirmed the successful inclusion of the phenolic compounds in bio-HDPE, though their interaction with the green polyolefin matrix was low. The mechanical performance of the bio-HDPE films was nearly unaffected by the natural compounds, presenting in all cases a ductile behavior. Interestingly, the phenolic compounds successfully increased the thermo-oxidative stability of bio-HDPE, yielding GA and QUER the highest performance. In particular, using these phenolic compounds, the onset oxidation temperature (OOT) value was improved by 43 and 41.5 °C, respectively. Similarly, the oxidation induction time (OIT) value, determined in isothermal conditions at 210 °C, increased from 4.5 min to approximately 109 and 138 min. Furthermore, the onset degradation temperature in air of bio-HDPE, measured for the 5% of mass loss (T5%), was improved by up to 21 °C after the addition of NAR. Moreover, the GA- and CA-containing bio-HDPE films showed a high antioxidant activity in alcoholic solution due to their favored release capacity, which opens up novel opportunities in active food packaging. The improved antioxidant performance of these phenolic compounds was ascribed to the multiple presence of hydroxyl groups and aromatic heterocyclic rings that provide these molecules with the features to permit the delocalization and the scavenging of free radicals. Therefore, the here-tested phenolic compounds, in particular QUER, can represent a sustainable and cost-effective alternative of synthetic antioxidants in polymer and biopolymer formulations, for which safety and environmental issues have been raised over time.


2002 ◽  
Vol 39 (6) ◽  
pp. 1221-1230 ◽  
Author(s):  
Henri P Sangam ◽  
R Kerry Rowe

Laboratory-accelerated ageing tests have been conducted to examine the depletion of antioxidants from high-density polyethylene (HDPE) geomembranes as a result of their exposure to various environments. Samples of 2.0 mm thick geomembrane were exposed to air, water, and municipal solid waste (MSW) leachate at temperatures of 22, 40, 55, 70, and 85°C. At various time intervals, samples were collected and the oxidative induction time (OIT) was evaluated. The results indicated that the antioxidants are depleted at rates 1.6 to 2.4 times faster for samples in water than for air-exposed samples. For samples in leachate, the depletion is about 4 times faster than that in air and 1.6–3.2 times faster than that in water. Using these rates, it is estimated that if the geomembrane examined were used as an MSW landfill primary liner, it would take at least 40 years to deplete the antioxidants from the geomembrane at a temperature of 33°C and over 150 years at a temperature of 13°C.Key words: ageing, antioxidants, durability, oxidative induction time, HDPE geomembrane, antioxidant depletion time.


2003 ◽  
Vol 774 ◽  
Author(s):  
Susan M. Rea ◽  
Serena M. Best ◽  
William Bonfield

AbstractHAPEXTM (40 vol% hydroxyapatite in a high-density polyethylene matrix) and AWPEX (40 vol% apatite-wollastonite glass ceramic in a high density polyethylene matrix) are composites designed to provide bioactivity and to match the mechanical properties of human cortical bone. HAPEXTM has had clinical success in middle ear and orbital implants, and there is great potential for further orthopaedic applications of these materials. However, more detailed in vitro investigations must be performed to better understand the biological interactions of the composites and so the bioactivity of each material was assessed in this study. Specifically, the effects of controlled surface topography and ceramic filler composition on apatite layer formation in acellular simulated body fluid (SBF) with ion concentration similar to those of human blood plasma were examined. Samples were prepared as 1 cm × 1 cm × 1 mm tiles with polished, roughened, or parallel-grooved surface finishes, and were incubated in 20 ml of SBF at 36.5 °C for 1, 3, 7, or 14 days. The formation of a biologically active apatite layer on the composite surface after immersion was demonstrated by thin-film x-ray diffraction (TF-XRD), environmental scanning electron microscopy (ESEM) imaging and energy dispersive x-ray (EDX) analysis. Variations in sample weight and solution pH over the period of incubation were also recorded. Significant differences were found between the two materials tested, with greater bioactivity in AWPEX than HAPEXTM overall. Results also indicate that within each material the surface topography is highly important, with rougher samples correlated to earlier apatite formation.


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